List of variants in gene KBTBD13 reported as benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001101362.3(KBTBD13):c.1200T>C (p.Gly400=)	rs2919360	0.99001
NM_001101362.3(KBTBD13):c.798A>G (p.Glu266=)	rs2919359	0.86820
NM_001101362.3(KBTBD13):c.242C>T (p.Ala81Val)	rs2919358	0.46622
NM_001101362.3(KBTBD13):c.378G>T (p.Ala126=)	rs2946642	0.45129
NM_001101362.3(KBTBD13):c.954C>G (p.Thr318=)	rs368781046	0.00246
NM_001101362.3(KBTBD13):c.1077A>G (p.Gly359=)	rs199526404	0.00224

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